Bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG / pramoxine hydrochlo... — RxCUI 2055751
RxNorm drug concept · Semantic clinical drug
RxCUI 2055751
Semantic clinical drug · SCD
● Current RxNorm concept 3 FDA products
3 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI2055751
Official nameBacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asbacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT / pramoxine HCl 10 MG per GM Topical Ointment
FDA products mapped3
Package NDCs mapped3
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Bacitracin Topical: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It is first aid to help prevent infection in minor cuts, scrapes, and burns. One cream product also has directions for athlete's foot, ringworm and jock itch.
- Clean the area, then put on a small amount, about the size of your fingertip. Do this 1 to 3 times a day, and you can cover it with a sterile bandage. One cream product is used as...
- Not longer than 1 week unless a doctor tells you to. If the problem is not getting better or gets worse, stop and check with a doctor.
- Stop if you get a rash or any allergic reaction, and talk to a doctor. Don't use it if you are allergic to any ingredient.
🕸️ Concept Web — How Bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG /... Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment
RxCUI 2055751 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 6
The active substance itself — no strength, form, or brand attached yet.
-
Bacitracin
1291IN -
Neomycin
7299IN -
Polymyxin B
8536IN -
Pramoxine
34347IN -
Bacitracin / neomycin / polymyxin B / pramoxine
466540MIN -
Pramoxine hydrochloride
57555PIN
-
Bacitracin
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Bacitracin / neomycin / polymyxin B / pramoxine Topical Ointment
374798SCDF -
Bacitracin / neomycin / polymyxin B / pramoxine hydrochloride Topical Ointment
2645927SCDFP -
Bacitracin / neomycin / polymyxin B / pramoxine Topical Product
1155349SCDG -
Bacitracin / neomycin / polymyxin B / pramoxine hydrochloride Topical Product
2662300SCDGP -
Topical Ointment
316985DF -
Topical Product
1151122DFG
-
Bacitracin / neomycin / polymyxin B / pramoxine Topical Ointment
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Bacitracin 0.5 UNT/MG
315454SCDC -
Neomycin 0.0035 MG/MG
328185SCDC -
Polymyxin B 5 UNT/MG
335956SCDC -
Pramoxine hydrochloride 0.01 MG/MG
995190SCDC
-
Bacitracin 0.5 UNT/MG
Showing up to 8 concepts per family — 16 of 16 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
-
Bacitracin 0.5 UNT/MG
SCDC · 315454 -
Neomycin 0.0035 MG/MG
SCDC · 328185 -
Polymyxin B 5 UNT/MG
SCDC · 335956 -
Pramoxine hydrochloride 0.01 MG/MG
SCDC · 995190 -
Bacitracin / neomycin / polymyxin B / pramoxine Topical Ointment
SCDF · 374798 -
Bacitracin / neomycin / polymyxin B / pramoxine hydrochloride Topical Ointment
SCDFP · 2645927 -
Bacitracin / neomycin / polymyxin B / pramoxine Topical Product
SCDG · 1155349 -
Bacitracin / neomycin / polymyxin B / pramoxine hydrochloride Topical Product
SCDGP · 2662300
📦 FDA Products & Package NDCs
3 products · 3 package NDCs
3 package NDCs map to RxCUI 2055751 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 61010-4401-01 | 28.4 g in 1 TUBE (61010-4401-1) | Triple Antibiotic with Pain Relief | Safetec of America, Inc. | 2019-11-01 |
| 69729-0615-05 | 1 TUBE in 1 BOX (69729-615-05) / 14 g in 1 TUBE (69729-615-... | PENIMIXCINA | OPMX LLC | 2018-09-05 |
| 69729-0616-61 | 1 TUBE in 1 BOX (69729-616-61) / 14 g in 1 TUBE (69729-616-... | PENTREXCILINA TRIPLE ANTIBIOTIC PLUS PAIN RELIEF | OPMX LLC | 2018-09-05 |
Observed labelers:
OPMX LLC (2) ·
Safetec of America, Inc. (1)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.